HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500121Generated: October 25, 2026
6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amine → 6-((2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl)methyl)quinoline
https://huagongshe.com/reaction/500121
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amine | HCID 57516523 | — |
| Reactant | 2-Chloro-3-(quinolin-6-yl)propanal | HCID 57516537 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-((2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl)methyl)quinoline | HCID 57971188 | — |
Reaction Steps
A mixture of 6-(4-bromo-3-fluorophenyl)-1,2,4-triazin-3-amine (800 mg, 2.97 mmol) and 2-chloro-3-quinolin-6-ylpropanal (784 mg, 3.57 mmol) in isopropyl alcohol (10.0 mL) in a sealed tube was heated at 110° C. for 48 h. After the reaction mixture was cooled to ambient temperature, the product was precipitated and collected by filtration. The mother liquor was concentrated and the residue was dissolved in ethyl acetate, washed with aqueous sodium bicarbonate, water, brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified on a silica gel column with methanol in dichloromethane (0-6%) to give the desired product. (65%) LCMS: (M+H)=434.0/436.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767675B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-a8fcf12b5a9945f4bc7fd8996d67fe46 |
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| Source note | uspto-grants-2010_08 |
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